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1. Um171
2. 1448724-09-1
3. Um-171
4. 8xz4j0ks9c
5. ((1r, 4r)-n1-(2-benzyl-7-(2-methyl-2h-tetrazol-5-yl)-9h-pyrimido(4,5-b)indol-4-yl)cyclohexane-1,4-diamine
6. 1,4-cyclohexanediamine, N1-(7-(2-methyl-2h-tetrazol-5-yl)-2-(phenylmethyl)-9h-pyrimido(4,5-b)indol-4-yl)-, Trans-
7. Trans-n1-(7-(2-methyl-2h-tetrazol-5-yl)-2-(phenylmethyl)-9h-pyrimido(4,5-b)indol-4-yl)-1,4-cyclohexanediamine
8. Trans-n1-[7-(2-methyl-2h-tetrazol-5-yl)-2-(phenylmethyl)-9h-pyrimido[4,5-b]indol-4-yl]-1,4-cyclohexanediamine
9. Um 171
10. Unii-8xz4j0ks9c
11. Um 171(discontinued Product)
12. Chembl4535214
13. Schembl15151854
14. Schembl18096437
15. Schembl20953135
16. Schembl23552414
17. Um-171 Pound>>um 171
18. Dtxsid201108994
19. Bcp23874
20. Yhc72409
21. S7608
22. Zinc299817087
23. Ccg-269273
24. Cs-7617
25. Ncgc00384196-02
26. Hy-12878
27. J3.577.659a
Molecular Weight | 453.5 g/mol |
---|---|
Molecular Formula | C25H27N9 |
XLogP3 | 4.5 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 5 |
Exact Mass | 453.23894190 g/mol |
Monoisotopic Mass | 453.23894190 g/mol |
Topological Polar Surface Area | 123 Ų |
Heavy Atom Count | 34 |
Formal Charge | 0 |
Complexity | 665 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Um171 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Um171 manufacturer or Um171 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Um171 manufacturer or Um171 supplier.
PharmaCompass also assists you with knowing the Um171 API Price utilized in the formulation of products. Um171 API Price is not always fixed or binding as the Um171 Price is obtained through a variety of data sources. The Um171 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Um171 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Um171, including repackagers and relabelers. The FDA regulates Um171 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Um171 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Um171 supplier is an individual or a company that provides Um171 active pharmaceutical ingredient (API) or Um171 finished formulations upon request. The Um171 suppliers may include Um171 API manufacturers, exporters, distributors and traders.
Um171 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Um171 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Um171 GMP manufacturer or Um171 GMP API supplier for your needs.
A Um171 CoA (Certificate of Analysis) is a formal document that attests to Um171's compliance with Um171 specifications and serves as a tool for batch-level quality control.
Um171 CoA mostly includes findings from lab analyses of a specific batch. For each Um171 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Um171 may be tested according to a variety of international standards, such as European Pharmacopoeia (Um171 EP), Um171 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Um171 USP).